EP2055748B1 - Farbstarkes c.i. pigment rot 254 und herstellungsverfahren dafür - Google Patents

Farbstarkes c.i. pigment rot 254 und herstellungsverfahren dafür Download PDF

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Publication number
EP2055748B1
EP2055748B1 EP07790612.1A EP07790612A EP2055748B1 EP 2055748 B1 EP2055748 B1 EP 2055748B1 EP 07790612 A EP07790612 A EP 07790612A EP 2055748 B1 EP2055748 B1 EP 2055748B1
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EP
European Patent Office
Prior art keywords
pigment
aprotic polar
parts
organic solvent
polar organic
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
EP07790612.1A
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English (en)
French (fr)
Other versions
EP2055748A1 (de
EP2055748A4 (de
Inventor
Hirotsugu Nemoto
Shousaburou Tanaka
Takashi Sato
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
DIC Corp
Original Assignee
DIC Corp
Dainippon Ink and Chemicals Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
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Publication date
Application filed by DIC Corp, Dainippon Ink and Chemicals Co Ltd filed Critical DIC Corp
Publication of EP2055748A1 publication Critical patent/EP2055748A1/de
Publication of EP2055748A4 publication Critical patent/EP2055748A4/de
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Publication of EP2055748B1 publication Critical patent/EP2055748B1/de
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Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
    • C09B67/0025—Crystal modifications; Special X-ray patterns
    • C09B67/003—Crystal modifications; Special X-ray patterns of diketopyrrolopyrrole
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B57/00—Other synthetic dyes of known constitution
    • C09B57/004—Diketopyrrolopyrrole dyes
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
    • C09B67/0001—Post-treatment of organic pigments or dyes
    • C09B67/0014—Influencing the physical properties by treatment with a liquid, e.g. solvents

Definitions

  • the present invention relates to a production method for a C. I. Pigment Red 254 coloring an object to be colored so as to have a higher chroma than coloring with conventional technology.
  • C. I. Pigment Red 254 pigments of various hues are known as an indicator with hue angle indicated by yellowish tint and blueish tint.
  • C. I. Pigment Red 254 which has stronger blueish tint and higher chroma is desired in the field of color coatings, plastics, and the like.
  • the conventional C. I. Pigment Red 254 was insufficient.
  • C. I. Pigment Red 254 obtained according to the present invention is more preferable within the specific surrounded region, and at the same time within the following specific surrounded region.
  • the liquid property of the aprotic polar organic solvent can not be expressed by pH. Therefore, for instance, in case of water which is previously humidifying the crude pigment, the liquid property of the aprotic polar organic solvent can be controlled by substituting pH for the starting point of conditioning by the amount of alkali, as from neutral to weak alkaline, then from weak alkaline to strong alkaline. Namely, alkali is so added to the aprotic polar organic solvent in order to make the basicity of the object to be heated higher than that before alkali is added.
  • the period of adding alkali is preferable, in order to make additional effect maximize, from one hour after the start of heating to one hour before the finish of heating. It is most preferable to perform prior conditioning at 100 - 130 °C for 2 - 10 hours, then to perform conditioning by heating in strong alkaline aprotic polar organic solvent after that, on the whole, in the range at 100 - 130 °C and for 3 - 7 hours.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Paints Or Removers (AREA)

Claims (2)

  1. Herstellungsverfahren für C. I. Pigment Rot 254, umfassend ein Heizverfahren mit 1,4-Diketo-3,6-bis(4-chlorphenyl)pyrrolo[3,4-c]pyrrol mit einem mittleren Teilchendurchmesser von 0,10 µm oder mehr und weniger als 0,20 µm in einem stark alkalischen aprotischen polaren organischen Lösungsmittel bei 100-130 °C für 2-10 Stunden, welches den Schritt umfasst:
    vorheriges Erhitzen bei 100-130°C in neutralem oder schwächer alkalischem aprotischem polarem organischen Lösungsmittel vor dem Heizverfahren, wobei
    dermittlere Teilchendurchmesser letztendlich 0,30-0,80 µm beträgt, wobei der Gehalt an Alkali, enthalten in dem neutralen oder schwächer alkalischen aprotischen polaren organischen Lösungsmittel zuvor, d.h. vor dem zweiten Heizverfahren, 0 - 0,07 Teile pro 100 Teile des aprotischen polaren organischen Lösungsmittels per Masseumsatz beträgt, und wobei danach das Alkali nach und nach zugegeben wird, sodass der Alkaligehalt in dem stark alkalischen aprotischen polaren organischen Lösungsmittel 0,02 - 0,15 Teile pro 100 Teile des aprotischen polaren Lösungsmittels nach Masseumsatz beträgt.
  2. Herstellungsverfahren für C. I. Pigment Rot 254 gemäß Anspruch 1, wobei das aprotische polare organische Lösungsmittel ein hydrophiles aprotisches polares organisches Lösungsmittel mit stickstoffhaltigem heterocyclischemRing ist, unddas Alkali ist ein anorganisches Alkali, das löslich in dem aprotischen polaren organischen Lösungsmittel und wasserlöslich ist.
EP07790612.1A 2006-07-20 2007-07-11 Farbstarkes c.i. pigment rot 254 und herstellungsverfahren dafür Active EP2055748B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2006198025 2006-07-20
PCT/JP2007/063808 WO2008010443A1 (en) 2006-07-20 2007-07-11 High-chroma c.i. pigment red 254 and process for producing the same

Publications (3)

Publication Number Publication Date
EP2055748A1 EP2055748A1 (de) 2009-05-06
EP2055748A4 EP2055748A4 (de) 2011-08-24
EP2055748B1 true EP2055748B1 (de) 2013-04-17

Family

ID=38956776

Family Applications (1)

Application Number Title Priority Date Filing Date
EP07790612.1A Active EP2055748B1 (de) 2006-07-20 2007-07-11 Farbstarkes c.i. pigment rot 254 und herstellungsverfahren dafür

Country Status (5)

Country Link
US (1) US7837784B2 (de)
EP (1) EP2055748B1 (de)
JP (1) JP4214493B2 (de)
CN (1) CN101490177B (de)
WO (1) WO2008010443A1 (de)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10048415B2 (en) 2007-08-12 2018-08-14 Toyota Motor Engineering & Manufacturing North America, Inc. Non-dichroic omnidirectional structural color
US10788608B2 (en) 2007-08-12 2020-09-29 Toyota Jidosha Kabushiki Kaisha Non-color shifting multilayer structures
US10690823B2 (en) 2007-08-12 2020-06-23 Toyota Motor Corporation Omnidirectional structural color made from metal and dielectric layers
US9612369B2 (en) 2007-08-12 2017-04-04 Toyota Motor Engineering & Manufacturing North America, Inc. Red omnidirectional structural color made from metal and dielectric layers
US10870740B2 (en) 2007-08-12 2020-12-22 Toyota Jidosha Kabushiki Kaisha Non-color shifting multilayer structures and protective coatings thereon
US9739917B2 (en) 2007-08-12 2017-08-22 Toyota Motor Engineering & Manufacturing North America, Inc. Red omnidirectional structural color made from metal and dielectric layers
DE102008032090A1 (de) * 2008-07-08 2010-01-14 Clariant International Ltd. PR 254-Pigmentzubereitung zur Verwendung in Colorfiltern
CN101831197A (zh) * 2010-05-17 2010-09-15 南通市争妍颜料化工有限公司 颜料红254的高遮盖力品种hl的生产工艺
US9678260B2 (en) 2012-08-10 2017-06-13 Toyota Motor Engineering & Manufacturing North America, Inc. Omnidirectional high chroma red structural color with semiconductor absorber layer
US9658375B2 (en) 2012-08-10 2017-05-23 Toyota Motor Engineering & Manufacturing North America, Inc. Omnidirectional high chroma red structural color with combination metal absorber and dielectric absorber layers
US9664832B2 (en) 2012-08-10 2017-05-30 Toyota Motor Engineering & Manufacturing North America, Inc. Omnidirectional high chroma red structural color with combination semiconductor absorber and dielectric absorber layers
CN102964865A (zh) * 2012-11-23 2013-03-13 江苏双乐化工颜料有限公司 一种颜料红254的制备方法
DE112015001639B4 (de) 2014-04-01 2023-12-14 Toyota Jidosha Kabushiki Kaisha Nicht-farbverschiebende mehrschichtige strukturen
US9810824B2 (en) 2015-01-28 2017-11-07 Toyota Motor Engineering & Manufacturing North America, Inc. Omnidirectional high chroma red structural colors
CN119907833A (zh) 2022-11-10 2025-04-29 Dic株式会社 吡咯并吡咯二酮化合物

Family Cites Families (17)

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JPS6442482U (de) 1987-09-09 1989-03-14
US4992101A (en) * 1988-04-15 1991-02-12 Ciba-Geigy Corporation Process for the preparation of opaque diketopyrrolo-pyrrole pigments
DE58908954D1 (de) 1988-04-15 1995-03-16 Ciba Geigy Ag Verfahren zur Herstellung deckender Diketopyrrolopyrrolpigmente.
US4895948A (en) 1988-06-20 1990-01-23 Ciba-Geigy Corporation Process for preparation of opaque quinacridones
US5229515A (en) * 1991-06-07 1993-07-20 Ciba-Geigy Corporation Process for preparing modified β-quinacridone pigment
JPH04372632A (ja) 1991-06-21 1992-12-25 Nippon Kayaku Co Ltd ポリオレフィン系樹脂用着色剤及びそれにより着色されたポリオレフィン系樹脂着色物
US5383966A (en) 1992-12-23 1995-01-24 Miles Inc. Process for the preparation of dispersible quinacridones
US5492564A (en) 1994-03-16 1996-02-20 Ciba-Geigy Corporation Diketopyrrolopyrrole pigment with high chroma
TW434296B (en) * 1994-10-12 2001-05-16 Ciba Sc Holding Ag Process for the preparation of diaryldiketopyrrolopyrrole pigments
US6063182A (en) * 1997-09-08 2000-05-16 Ciba Speciality Chemicals Corporation Stir-in pigment compositions
IN220164B (de) * 1997-09-08 2008-07-11 Ciba Geigy Ag
ES2370485T3 (es) * 1999-07-09 2011-12-16 Basf Se C.i. pigmento red 254 con propiedades colorantes mejoradas.
DE10028104A1 (de) * 2000-06-07 2001-12-13 Clariant Gmbh Verfahren zur Herstellung von Diketopyrrologyrrol-Pigmenten
DE10031558A1 (de) 2000-06-28 2002-01-10 Clariant Gmbh Verfahren zur Konditionierung von organischen Pigmenten
AU2002342633A1 (en) 2001-09-11 2003-03-24 Ciba Specialty Chemicals Holding Inc. Process for the preparation of diketopyrrolopyrroles
MXPA05008832A (es) * 2003-02-20 2005-10-05 Ciba Sc Holding Ag Composicion de pigmento facilmente dispersable.
JP2006206759A (ja) 2005-01-28 2006-08-10 Dainippon Ink & Chem Inc ジケトピロロピロール系顔料の製造方法

Also Published As

Publication number Publication date
CN101490177B (zh) 2013-07-17
EP2055748A1 (de) 2009-05-06
JPWO2008010443A1 (ja) 2009-12-17
JP4214493B2 (ja) 2009-01-28
US20090241802A1 (en) 2009-10-01
EP2055748A4 (de) 2011-08-24
WO2008010443A1 (en) 2008-01-24
US7837784B2 (en) 2010-11-23
CN101490177A (zh) 2009-07-22

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